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B6.Cg-Tyr c−2J Hr hr /J mice have a stronger delayed sunburn reaction and are good for UV research.

Rhupus is a complex syndrome that combines rheumatoid arthritis and lupus, making diagnosis challenging.

A circular RNA helps cashmere goat hair cells become hair follicles by blocking a molecule to boost a gene important for hair growth.

Rapamycin treatment helps with mitochondrial disease by reducing PKC levels.

Mutations in the Sgk3 gene cause fuzzy hair in mice.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

RIPK1 inhibitors may help prevent alopecia areata by reducing immune cell activity.

Key genes and RNA networks regulate hair growth and follicle density in Rex rabbits.

FCER1A and RGS1 may help diagnose and treat systemic lupus erythematosus.

Most Recessive Dystrophic Epidermolysis Bullosa patients with a specific mutation likely have Sephardic ancestry from about 500 years ago.

Reducing SFRP1 can promote hair growth and may help treat hair loss.

DKK4 can be used to improve wool quality in Zhexi Angora rabbits.

Msx2 is essential for proper enamel formation by preventing abnormal cell transformation.

Deleting Rac1 in the skin depletes stem cells and damages hair follicles.

RORA may help regulate hair growth by affecting hair follicle stem cells.

Removing SIX1 in fat cells reduces skin fibrosis.

As skin cells mature, vitamin D receptor levels decrease while retinoid X receptor α levels increase.

A new keratin, hK6irs1, is found in all layers of the hair follicle's inner root sheath.

SQSTM1 is linked to increased risk of alopecia areata.

NCSTN gene mutation causes abnormal skin cell differentiation and more inflammation, contributing to Hidradenitis Suppurativa.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

Identical twins with a rare KRT 86 gene mutation both have the hair disorder monilethrix.

H3K4me3 helps control RSPO3 to influence hair growth and development.

The tumor suppressor BRCA2 helps in cell division by bringing key proteins to the area where cells split.

Olmsted syndrome can be inherited as an autosomal recessive trait due to a rare TRPV3 gene mutation.

Thioredoxin reductase 1 does not affect glucocorticoid receptor activity in hair follicle cells.

RPGRIP1L helps skin cells stick together by blocking PKCβII, which can prevent skin blistering like in pemphigus.